Back to Search
Start Over
X-linked Malformation Deafness : Neurodevelopmental Symptoms Are Common in Children With IP3 Malformation and Mutation in POU3F4
- Source :
- Ear and Hearing
- Publication Year :
- 2022
- Publisher :
- Linköpings universitet, Institutionen för beteendevetenskap och lärande, 2022.
-
Abstract
- Supplemental Digital Content is available in the text.<br />Objective: Incomplete partition type 3 (IP3) malformation deafness is a rare hereditary cause of congenital or rapid progressive hearing loss. The children present with a severe to profound mixed hearing loss and temporal bone imaging show a typical inner ear malformation classified as IP3. Cochlear implantation is one option of hearing restoration in severe cases. Little is known about other specific difficulties these children might exhibit, for instance possible neurodevelopmental symptoms. Material and methods: Ten 2; 0 to 9; 6-year-old children with IP3 malformation deafness (nine boys and one girl) with cochlear implants were evaluated with a retrospective chart review in combination with an additional extensive multidisciplinary assessment day. Hearing, language, cognition, and mental ill-health were compared with a control group of ten 1; 6 to 14; 5-year-old children with cochlear implants (seven boys and three girls) with another genetic cause of deafness, mutations in the GJB2 gene. Results: Mutations in POU3F4 were found in nine of the 10 children with IP3 malformation. Children with IP3 malformation deafness had an atypical outcome with low level of speech recognition (especially in noise), executive functioning deficits, delayed or impaired speech as well as atypical lexical-semantic and pragmatic abilities, and exhibited mental ill-health issues. Parents of children with IP3 malformation were more likely to report that they were worried about their child’s psychosocial wellbeing. Controls, however, had more age-typical results in all these domains. Eight of 10 children in the experimental group had high nonverbal cognitive ability despite their broad range of neurodevelopmental symptoms. Conclusions: While cochlear implantation is a feasible alternative for children with IP3 malformation deafness, co-occurring neurodevelopmental anomalies, such as attention deficit hyperactivity or developmental language disorder, and mental ill-health issues require an extensive and consistent multidisciplinary team approach during childhood to support their overall habilitation.
- Subjects :
- Male
medicine.medical_specialty
Adolescent
Hearing loss
media_common.quotation_subject
education.educational_degree
Oto-rino-laryngologi
Audiology
Deafness
Habilitation
Incomplete partition type 3
Speech and Hearing
Nonverbal communication
Developmental language disorder
Chart review
Temporal bone
otorhinolaryngologic diseases
Medicine
Humans
ADHD
Girl
education
Child
X-linked malformation deafness
media_common
Retrospective Studies
business.industry
Cognition
Syndrome
Cochlear Implantation
POU3F4
Cochlear implantation
Cochlear Implants
Otorhinolaryngology
Child, Preschool
Mutation
POU Domain Factors
ComputingMethodologies_DOCUMENTANDTEXTPROCESSING
Female
Mental health
medicine.symptom
business
Psychosocial
Research Article
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Ear and Hearing
- Accession number :
- edsair.doi.dedup.....aba7a2d6a3dd3f1ba7c4a8d202bb0aaa